WNT signaling suppresses oligodendrogenesis via Ngn2-dependent direct inhibition of Olig2 expression
Olig2 transcription factor is essential for the maintenance of neural progenitor cells (NPCs) in the pMN domain and their sequential specification into motor neurons (MNs) and oligodendrocyte precursor cells (OPCs). The expression of Olig2 rapidly declines in newly generated MNs. However, Olig2 expr...
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Veröffentlicht in: | Molecular brain 2020-11, Vol.13 (1), p.1-155, Article 155 |
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Sprache: | eng |
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Zusammenfassung: | Olig2
transcription factor is essential for the maintenance of neural progenitor cells (NPCs) in the pMN domain and their sequential specification into motor neurons (MNs) and oligodendrocyte precursor cells (OPCs). The expression of
Olig2
rapidly declines in newly generated MNs. However,
Olig2
expression persists in later-born OPCs and antagonizes the expression of MN-related genes. The mechanism underlying the differential expression of
Olig2
in MNs and oligodendrocytes remains unknown. Here, we report that activation of WNT/β-catenin signaling in pMN lineage cells abolished
Olig2
expression coupled with a dramatic increase of
Ngn2
expression. Luciferase reporter assay showed that
Ngn2
inhibited
Olig2
promoter activity. Overexpression of Ngn2-EnR transcription repressor blocked the expression of
Olig2
in ovo. Our results suggest that down-regulation of WNT-
Ngn2
signaling contributes to oligodendrogenesis from the pMN domain and the persistent
Olig2
expression in OPCs. |
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ISSN: | 1756-6606 1756-6606 |
DOI: | 10.1186/s13041-020-00696-0 |